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NCT04686929

Abatacept s.c. for aGVHD Prevention in Haplo-HCT

Status unknown Phase 1, PHASE2 Last updated 20 December 2022
What this trial tests

Phase 1, PHASE2 trial testing Abatacept s.c. in Abatacept in 29 participants. Status unknown.

Timeline
1 June 2021
Primary endpoint
30 June 2023
30 December 2023

Quick facts

Lead sponsorThe First Affiliated Hospital of Soochow University
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment29
Start date1 June 2021
Primary completion30 June 2023
Estimated completion30 December 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

The First Affiliated Hospital of Soochow University

Who can join

18 and older, any sex, with Abatacept or Acute-graft-versus-host Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Acute graft-versus-host disease (aGVHD) is a potentially fatal complication after allogeneic hematopoietic cell transplantation (HCT), particularly for that with a HLA-mismatched donor. Abatacept has been demonstrated as a potent drug to reduce the risk of aGVHD, but the efficacy of subcutaneous form has yet been investigated. This trial is designed to preliminarily determin the efficacy and saftey of subcutaneous abatacept in the prevention of aGVHD after haplo-identical HCT.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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